2016
DOI: 10.1080/17425247.2016.1227783
|View full text |Cite
|
Sign up to set email alerts
|

Recent perspectives on the delivery of biologics to back of the eye

Abstract: Introduction Biologics are generally macromolecules, large in size with poor stability in biological environments. Delivery of biologics to tissues at the back of the eye remains a challenge. To overcome these challenges and treat posterior ocular diseases, several novel approaches have been developed. Nanotechnology-based delivery systems, like drug encapsulation technology, macromolecule implants and gene delivery are under investigation. We provide an overview of emerging technologies for biologics delivery… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
36
0

Year Published

2017
2017
2022
2022

Publication Types

Select...
6
2

Relationship

1
7

Authors

Journals

citations
Cited by 51 publications
(36 citation statements)
references
References 141 publications
0
36
0
Order By: Relevance
“…Therefore, it is not surprising that crystallin-based cell survival strategies have been proposed to protect and rescue RGCs from degeneration associated with glaucomatous and other optic neuropathies [50]. However, therapeutic protein delivery to the retina faces many obstacles [66][67][68] compared to small molecule therapy such as E 2 delivered topically [20], which would induce the desired changes in protein expression.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, it is not surprising that crystallin-based cell survival strategies have been proposed to protect and rescue RGCs from degeneration associated with glaucomatous and other optic neuropathies [50]. However, therapeutic protein delivery to the retina faces many obstacles [66][67][68] compared to small molecule therapy such as E 2 delivered topically [20], which would induce the desired changes in protein expression.…”
Section: Discussionmentioning
confidence: 99%
“…For instance, the average apparent plasma half-life of pegaptanib is 10 days after 3 mg dose whereas ranibizumab remains for 2.88 days in rabbit. Half-life of bevacizumab is 4.32 days with maximum concentration 162 μg/ml in vitreous cavity [66]. In AMD, the vitreous elimination of ranizumab is just 9 days and intrinsic systemic elimination half-life is 2 hours followed by multiple intravitreal injection dose of 0.3–2.0 mg/eye biweekly or monthly [17].…”
Section: Proteins and Peptides: Challenges In Ocular Deliverymentioning
confidence: 99%
“…23 Posterior segment diseases such as macular degeneration and retinopathy cannot currently be treated with topical vehicles and require more invasive techniques such as direct injections or surgical interventions. 24, 25 …”
Section: Anatomy and Physiology Of The Eyementioning
confidence: 99%